Abstract
The stable benzylazido-boronate ester 1 is presented as an example of a dual-functional linker that allows the synthetically valuable boronate motif to be clicked onto other molecules under mild conditions. The utility of the azido-boronate motif as a modular building block is demonstrated in the rapid synthesis of drug-like structures employing sequential catalytic azide-alkyne cycloaddition and Suzuki coupling reactions.
Original language | English |
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Pages (from-to) | 3913-3917 |
Number of pages | 5 |
Journal | TETRAHEDRON LETTERS |
Volume | 51 |
Issue number | 30 |
DOIs | |
Publication status | Published - 28 Jul 2010 |